Canonical Allele Identifier: CA445964617

Gene: SLC25A46

Linked Data

• dbSNP Id: rs1800255650
• MyVariant Identifiers: chr5:g.110097389G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761689G>A , CM000667.2:g.110761689G>A	GRCh38
NC_000005.9:g.110097389G>A , CM000667.1:g.110097389G>A	GRCh37
NC_000005.8:g.110125288G>A	NCBI36
NG_051334.1:g.28554G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1164G>A MANE Select	ENSP00000348211.3:p.Gly388=
ENST00000355943.7:c.1164G>A	ENSP00000348211.3:p.Gly388=
ENST00000447245.6:c.921G>A	ENSP00000399717.2:p.Gly307=
ENST00000504098.1:c.726G>A	ENSP00000425708.1:p.Gly242=
ENST00000509432.1:c.525G>A	ENSP00000426604.1:p.Gly175=
ENST00000513706.2:n.2764G>A
ENST00000513807.5:c.678G>A	ENSP00000421134.1:p.Gly226=
NM_001303249.1:c.921G>A	NP_001290178.1:p.Gly307=
NM_001303250.1:c.891G>A	NP_001290179.1:p.Gly297=
NM_138773.2:c.1164G>A	NP_620128.1:p.Gly388=
NM_001303249.2:c.921G>A	NP_001290178.1:p.Gly307=
NM_001303250.2:c.891G>A	NP_001290179.1:p.Gly297=
NM_138773.3:c.1164G>A	NP_620128.1:p.Gly388=
NR_138151.1:n.1438G>A
NM_138773.4:c.1164G>A MANE Select	NP_620128.1:p.Gly388=
NM_001303249.3:c.921G>A	NP_001290178.1:p.Gly307=
NM_001303250.3:c.891G>A	NP_001290179.1:p.Gly297=
NR_138151.2:n.1403G>A